Catalyst, production process therefor and use thereof

a catalyst and catalyst technology, applied in the field of catalysts, processes for producing catalysts, can solve the problems of noble metals used on the cathode surface, high cost and limited amount of platinum, and the use of long-term durability in these applications, so as to achieve high oxygen reduction ability, not corroded, and high performance.

Inactive Publication Date: 2011-03-10
SHOWA DENKO KK
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

[0032]The catalysts according to the invention are stable and are not corroded in acidic electrolytes or at high potential, have high oxygen reducing

Problems solved by technology

The use in these applications requires long-term durability.
However, since platinum is expensive and exists in a limited amount, alternative catalysts have been desired.
Further, the noble metals used on a cathode surface are often dissolved in an acidic atmosphere and are not suited in applications requiring long-term durability.
However, the materials containing these nonmetals do not provide sufficient oxygen reducing ability for pr

Method used

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  • Catalyst, production process therefor and use thereof
  • Catalyst, production process therefor and use thereof
  • Catalyst, production process therefor and use thereof

Examples

Experimental program
Comparison scheme
Effect test

example 1

1. Preparation of Catalyst

[0117]Niobium (IV) oxide (NbO2) weighing 2.60 g (21 mmol) was mixed with 600 mg (50 mmol) of carbon (Vulcan 72 manufactured by Cabot Corporation) and was sufficiently crushed. The resultant powder mixture was heat treated in a tubular furnace under a nitrogen atmosphere at 1600° C. for 1 hour to give 2.55 g of niobium carbonitride.

[0118]The niobium carbonitride in an amount of 2.00 g was heated in the tubular furnace at 800° C. for 1 hour while passing an argon gas containing 1% by volume of oxygen gas. As a result, 2.15 g of niobium oxycarbonitride (hereinafter, also the catalyst (1)) was obtained.

[0119]The results of elemental analysis of the catalyst (1) are shown in Table 1. In the niobium oxycarbonitride (NbCxNyOz), x, y and z were 0.52, 0.43 and 0.78 respectively, x+y+z was 1.73, and 4x+3y+2z was 4.93.

2. Production of Fuel Cell Electrode

[0120]The oxygen reducing ability was determined in the following manner. The catalyst (1) in an amount of 0.095 g a...

example 2

1. Preparation of Catalyst

[0133]The procedures in Example 1 were repeated, except that the amount of carbon was changed from 600 mg to 480 mg (40 mmol), thereby producing 1.83 g of niobium carbonitride. The niobium carbonitride in an amount of 1.02 g was heated to give 1.09 g of niobium oxycarbonitride (hereinafter, also the catalyst (2)).

[0134]The results of elemental analysis of the catalyst (2) are shown in Table 1. In the niobium oxycarbonitride (NbCxNyOz), x, y and z were 0.32, 0.44 and 0.78 respectively, x+y+z was 1.54, and 4x+3y+2z was 4.16.

2. Production of Fuel Cell Electrode

[0135]A fuel cell electrode (2) was produced in the same manner as in Example 1, except that the catalyst (2) was used.

3. Evaluation of Oxygen Reducing Ability

[0136]The fuel cell electrode (2) was evaluated for catalytic performance (oxygen reducing ability) as described in Example 1.

[0137]The current-potential curve recorded during the measurement is shown in FIG. 2.

[0138]Table 2 shows the evaluation re...

example 3

1. Preparation of Catalyst

[0140]The procedures in Example 1 were repeated, except that the amount of carbon was changed from 600 mg to 730 mg (61 mmol), thereby producing 1.67 g of niobium carbonitride. The niobium carbonitride in an amount of 1.10 g was heated to give 1.12 g of niobium oxycarbonitride (hereinafter, also the catalyst (3)).

[0141]The results of elemental analysis of the catalyst (3) are shown in Table 1. In the niobium oxycarbonitride (NbCxNyOz), x, y and z were 0.55, 0.41 and 0.77 respectively, x+y+z was 1.73, and 4x+3y+2z was 4.97.

2. Production of Fuel Cell Electrode

[0142]A fuel cell electrode (3) was produced in the same manner as in Example 1, except that the catalyst (3) was used.

3. Evaluation of Oxygen Reducing Ability

[0143]The fuel cell electrode (3) was evaluated for catalytic performance (oxygen reducing ability) as described in Example 1.

[0144]The current-potential curve recorded during the measurement is shown in FIG. 3.

[0145]Table 2 shows the evaluation re...

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Abstract

Catalysts of the invention are not corroded in acidic electrolytes or at high potential and have excellent durability and high oxygen reducing ability. The catalysts include a niobium oxycarbonitride represented by a compositional formula NbCxNyOz (wherein x, y and z represent a ratio of the numbers of the atoms, 0.05≦x<0.7, 0.01≦y<0.7, 0.4≦z<2.5, 1.0<x+y+z<2.56, and 4.0≦4x+3y+2z).

Description

FIELD OF THE INVENTION[0001]The present invention relates to catalysts, processes for producing the catalysts, and use of the catalysts.BACKGROUND OF THE INVENTION[0002]Fuel cells are classified into several types according to the electrolytes or electrodes used therein. Typical types are alkaline types, phosphoric acid types, molten carbonate types, solid electrolyte types and polymer electrolyte types. In particular, polymer electrolyte fuel cells that can operate at temperatures ranging from low temperatures (about −40° C.) to about 120° C. attract attention and are progressively developed and practically used as power sources for low pollution automobiles. The polymer electrolyte fuel cells are expected to be used as automobile drive sources or stationary power sources. The use in these applications requires long-term durability.[0003]The polymer electrolyte fuel cell has a solid polymer electrolyte sandwiched between an anode and a cathode. A fuel is fed to the anode, and oxyge...

Claims

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Application Information

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IPC IPC(8): H01M8/10H01M4/58
CPCB01J27/22B01J27/24H01M4/8828Y02E60/50H01M2008/1095H01M4/90H01M4/9016
Inventor MONDEN, RYUJIKUROZUMI, TADATOSHISHISHIKURA, TOSHIKAZU
Owner SHOWA DENKO KK
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